3-[(2,4-Dimethylpyrrol-5-yl)methylidenyl]-2-indolinon Chemical Properties

Melting point:

220-222℃

Density 

1.256

storage temp. 

2-8°C

InChI

InChI=1S/C15H14N2O/c1-9-7-10(2)16-14(9)8-12-11-5-3-4-6-13(11)17-15(12)18/h3-8,16H,1-2H3,(H,17,18)/b12-8-

InChIKey

WUWDLXZGHZSWQZ-WQLSENKSSA-N

SMILES

N1C2=C(C=CC=C2)/C(=C/C2=C(C)C=C(C)N2)/C1=O

3-[(2,4-Dimethylpyrrol-5-yl)methylidenyl]-2-indolinon Usage And Synthesis

Uses

Adrenalone is an adrenergic agonist.

Uses

Semaxanib is a potent and selective VEGFR(Flk-1/KDR) inhibitor.

Definition

ChEBI: An oxindole that is 3-methyleneoxindole in which one of the hydrogens of the methylene group is replaced by a 3,5-dimethylpyrrol-2-yl group.

Synthesis

GENERAL METHOD: 2-Indolone (200 mg, 1 eq.) was dissolved in methanol (5 mL) and piperidine (1.5 eq.) and 3,5-dimethyl-2-pyrrolecarboxaldehyde (1.2 eq.) were added sequentially. The reaction mixture was heated to reflux with continuous stirring for 1 to 4 hours. After completion of the reaction, it was cooled to room temperature. The reaction mixture was filtered and the resulting solid was washed three times with methanol. The solid product was collected and dried under vacuum to remove residual methanol to give the final target product (Z)-3-((3,5-dimethyl-1H-pyrrol-2-yl)methylene)dihydroindol-2-one.

References

[1] Journal of Antibiotics, 2018, vol. 71, # 10, p. 887 - 897
[2] Tetrahedron, 2009, vol. 65, # 25, p. 4894 - 4903
[3] ChemMedChem, 2016, vol. 11, # 1, p. 72 - 80
[4] Journal of Medicinal Chemistry, 1998, vol. 41, # 14, p. 2588 - 2603
[5] Synthetic Communications, 2008, vol. 38, # 17, p. 3017 - 3022

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